Abstract

Estimates of phosphorus (P) and nitrogen (N) gains and losses during annual macrophyte growth, death and 2 years decomposition were made along a gradient of surface water nutrient concentrations in the Florida Everglades. Annual rates of P and N allocation to growing leaves, translocation or leaching from dying leaves, and retention in dead leaves of Cladium jamaicense Crantz and Typha domingensis Pers. were correlated to soluble reactive P and nitrate concentrations in surface water. Rates of each of these processes were higher in T. domingensis than in C. jamaicense, Cladium jamaicense rates increased linearly along the nutrient gradients, but did not fluctuate with yearly variations in soluble reactive P or nitrate concentrations. For T. domingensis, annual rates were strongly correlated with mean annual soluble reactive P and nitrate concentrations during specific sampling years. Responses of C. jamaicense to the nutrient gradient were characteristic of species competitive in an infertile habitat, while responses of T. domingensis were characteristic of species competitive in a fertile habitat. The main effect of P and N enrichment on leaf nutrient flux was to accelerate translocation or leaching from dying tissue, rather than to increase retention in standing dead leaves. Freshly dead leaves retained only slightly greater quantities of P and N under enriched conditions in comparison to background conditions. After 2 years of decomposition, approximately half of the leaf litter mass remained intact. Increasing P and N concentrations in decomposing leaf litter resulted in net uptake or retention of these elements after 2 years despite decreasing litter mass. The total amounts of P and N that were sequestered annually by T. domingensis after processes of leaf production, mortality and 2 years decomposition were lowest under non-enriched conditions and reached a maximum under a moderate level of enrichment. Wetland ecosystems such as the Everglades, which developed under conditions of low nutrient supply, may offer a finite potential for accelerated nutrient retention when the exogenous nutrient supply increases as a result of human activities. However, a plant species such as C. jamaicense, that is adapted to a low-nutrient environment, may have a low nutrient threshold before it loses its competitive capability and its habitat is invaded by a species such as T. domingensis that is better adapted to a high-nutrient environment.

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